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ID

43663

Description

Optimal Anticoagulation for Higher Risk Patients Post-Catheter Ablation for Atrial Fibrillation Trial; ODM derived from: https://clinicaltrials.gov/show/NCT02168829

Lien

https://clinicaltrials.gov/show/NCT02168829

Mots-clés

  1. 25/04/2016 25/04/2016 -
  2. 20/09/2021 20/09/2021 -
Téléchargé le

20 septembre 2021

DOI

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Licence

Creative Commons BY 4.0

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    Eligibility Atrial Fibrillation NCT02168829

    Eligibility Atrial Fibrillation NCT02168829

    Inclusion Criteria
    Description

    Inclusion Criteria

    Alias
    UMLS CUI
    C1512693
    at least one year post-successful catheter ablation for af or left atrial arrhythmia. successful af ablation is defined as no af/afl/at >30 seconds on any pre-enrolment monitoring
    Description

    Cardiac ablation Atrial Fibrillation | Cardiac ablation Left atrial structure Cardiac Arrhythmia | Atrial Flutter

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0162563
    UMLS CUI [1,2]
    C0004238
    UMLS CUI [2,1]
    C0162563
    UMLS CUI [2,2]
    C0225860
    UMLS CUI [2,3]
    C0003811
    UMLS CUI [3]
    C0004239
    chads2 risk score of 1 or more. patients with chads2 score of 0, but who are >65 years old, or who are female with vascular disease will also be included
    Description

    Congestive heart failure, hypertension, age 75 years or older, diabetes, and previous stroke or transient ischemic attack risk score | Age | Female Vascular Diseases

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2585876
    UMLS CUI [2]
    C0001779
    UMLS CUI [3,1]
    C0086287
    UMLS CUI [3,2]
    C0042373
    > 18 years of age
    Description

    Age

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0001779
    Exclusion Criteria
    Description

    Exclusion Criteria

    Alias
    UMLS CUI
    C0680251
    does not meet all of the above listed inclusion criteria.
    Description

    Negation Inclusion

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C1518422
    UMLS CUI [1,2]
    C1512693
    unable or unwilling to provide informed consent.
    Description

    Unable Informed Consent

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C1299582
    UMLS CUI [1,2]
    C0021430
    included in another clinical trial
    Description

    Study Subject Participation Status

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C2348568
    gfr < 30 ml/min
    Description

    Glomerular Filtration Rate

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0017654
    contraindication to oral anticoagulation (oac)
    Description

    Medical contraindication Oral anticoagulants

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C1301624
    UMLS CUI [1,2]
    C0354604
    metallic prosthetic heart valve
    Description

    Metallic Heart Valve Prosthesis

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0018825
    UMLS CUI [1,2]
    C2986473
    non-arrhythmic condition necessitating long-term oac
    Description

    Disease Requirement Long-term oral anticoagulants

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C0012634
    UMLS CUI [1,2]
    C1514873
    UMLS CUI [1,3]
    C0354604
    UMLS CUI [1,4]
    C0443252
    stroke within one year prior to enrolment
    Description

    Cerebrovascular accident

    Type de données

    boolean

    Alias
    UMLS CUI [1]
    C0038454

    Similar models

    Eligibility Atrial Fibrillation NCT02168829

    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    C1512693 (UMLS CUI)
    Cardiac ablation Atrial Fibrillation | Cardiac ablation Left atrial structure Cardiac Arrhythmia | Atrial Flutter
    Item
    at least one year post-successful catheter ablation for af or left atrial arrhythmia. successful af ablation is defined as no af/afl/at >30 seconds on any pre-enrolment monitoring
    boolean
    C0162563 (UMLS CUI [1,1])
    C0004238 (UMLS CUI [1,2])
    C0162563 (UMLS CUI [2,1])
    C0225860 (UMLS CUI [2,2])
    C0003811 (UMLS CUI [2,3])
    C0004239 (UMLS CUI [3])
    Congestive heart failure, hypertension, age 75 years or older, diabetes, and previous stroke or transient ischemic attack risk score | Age | Female Vascular Diseases
    Item
    chads2 risk score of 1 or more. patients with chads2 score of 0, but who are >65 years old, or who are female with vascular disease will also be included
    boolean
    C2585876 (UMLS CUI [1])
    C0001779 (UMLS CUI [2])
    C0086287 (UMLS CUI [3,1])
    C0042373 (UMLS CUI [3,2])
    Age
    Item
    > 18 years of age
    boolean
    C0001779 (UMLS CUI [1])
    Item Group
    C0680251 (UMLS CUI)
    Negation Inclusion
    Item
    does not meet all of the above listed inclusion criteria.
    boolean
    C1518422 (UMLS CUI [1,1])
    C1512693 (UMLS CUI [1,2])
    Unable Informed Consent
    Item
    unable or unwilling to provide informed consent.
    boolean
    C1299582 (UMLS CUI [1,1])
    C0021430 (UMLS CUI [1,2])
    Study Subject Participation Status
    Item
    included in another clinical trial
    boolean
    C2348568 (UMLS CUI [1])
    Glomerular Filtration Rate
    Item
    gfr < 30 ml/min
    boolean
    C0017654 (UMLS CUI [1])
    Medical contraindication Oral anticoagulants
    Item
    contraindication to oral anticoagulation (oac)
    boolean
    C1301624 (UMLS CUI [1,1])
    C0354604 (UMLS CUI [1,2])
    Metallic Heart Valve Prosthesis
    Item
    metallic prosthetic heart valve
    boolean
    C0018825 (UMLS CUI [1,1])
    C2986473 (UMLS CUI [1,2])
    Disease Requirement Long-term oral anticoagulants
    Item
    non-arrhythmic condition necessitating long-term oac
    boolean
    C0012634 (UMLS CUI [1,1])
    C1514873 (UMLS CUI [1,2])
    C0354604 (UMLS CUI [1,3])
    C0443252 (UMLS CUI [1,4])
    Cerebrovascular accident
    Item
    stroke within one year prior to enrolment
    boolean
    C0038454 (UMLS CUI [1])

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